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>   home   >   Products   >   Peptides   >   Blocking Peptides   >   CFL2 Antibody (N-term) Blocking peptide   

CFL2 Antibody (N-term) Blocking peptide

Synthetic peptide

Product Information
Primary Accession Q9Y281
Clone Names 100507017
Peptide ID 100507017
Additional Information
Gene ID 1073
Other Names Cofilin-2, Cofilin, muscle isoform, CFL2
Target/Specificity The synthetic peptide sequence used to generate the antibody AP14117a was selected from the N-term region of CFL2. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Format Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
PrecautionsThis product is for research use only. Not for use in diagnostic or therapeutic procedures.
Protein Information
Name CFL2
Function Controls reversibly actin polymerization and depolymerization in a pH-sensitive manner. Its F-actin depolymerization activity is regulated by association with CSPR3 (PubMed:19752190). It has the ability to bind G- and F-actin in a 1:1 ratio of cofilin to actin. It is the major component of intranuclear and cytoplasmic actin rods. Required for muscle maintenance. May play a role during the exchange of alpha-actin forms during the early postnatal remodeling of the sarcomere (By similarity).
Cellular Location Nucleus matrix. Cytoplasm, cytoskeleton. Note=Colocalizes with CSPR3 in the Z line of sarcomeres.
Tissue Location Isoform CFL2b is expressed predominantly in skeletal muscle and heart. Isoform CFL2a is expressed in various tissues
Research Areas
Citations (0)

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This gene encodes an intracellular protein that isinvolved in the regulation of actin-filament dynamics. This proteinis a major component of intranuclear and cytoplasmic actin rods. Itcan bind G- and F-actin in a 1:1 ratio of cofilin to actin, and itreversibly controls actin polymerization and depolymerization in apH-dependent manner. Mutations in this gene cause nemaline myopathytype 7, a form of congenital myopathy. Alternative splicing resultsin multiple transcript variants.


Vogel, S., et al. J. Biol. Chem. 285(44):33756-33763(2010)Borensztajn, K., et al. Thromb. Res. 125 (6), E323-E328 (2010) :Papalouka, V., et al. Mol. Cell. Biol. 29(22):6046-6058(2009)Wu, Y., et al. Retrovirology 5, 95 (2008) :Agrawal, P.B., et al. Am. J. Hum. Genet. 80(1):162-167(2007)

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$ 80.00
Cat# BP14117a
Availability: In Stock
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